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calendar

19,880 catalysts · 4,728 grant · 3,350 8k filing · 2,768 device 510k · 2,721 approval · 2,000 device recall · 1,955 device pma

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  • grant4,728
  • 8k filing3,350
  • device 510k2,768
  • approval2,721
  • device recall2,000
  • device pma1,955
device adverse event
1,000
  • recall693
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Jul 28, 2025

    45
    ›Jul 31, 2025device 510k380d agoZimmer Biomet — Trabecular Metal Acetabular Revision System, Acetabular Liners and Constrained Liners (510k cleared)ZIMMER BIOMET HOLDINGS, INC.

    Product code: JDI. Advisory committee: Orthopedic. Type: Traditional

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoSiemens Medical Solutions USA, Inc. — Biograph Trinion (510k cleared)

    Product code: KPS. Advisory committee: Radiology. Type: Special

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoShenzhen TPH Technology Co., Ltd. — Wearable Breast Pump (Model FS12A); Wearable Breast Pump (Model FS12B) (510k cleared)Fortior Technology (Shenzhen) Co., Ltd./ADR

    Product code: HGX. Advisory committee: Obstetrics/Gynecology. Type: Special

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoHologic, Inc. — Genius AI Detection 2.0 (510k cleared)

    Product code: QDQ. Advisory committee: Radiology. Type: Traditional

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoRoche Molecular Systems, Inc. — cobas Respiratory 4-flex for use on the cobas 5800/6800/8800 Systems (510k cleared)

    Product code: QOF. Advisory committee: Microbiology. Type: Traditional

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoLutronic Corporation — eCO2 3D (510k cleared)

    Product code: ONG. Advisory committee: General, Plastic Surgery. Type: Traditional

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoMedacta International S.A. — NextAR(TM) Spine (510k cleared)Stemedica International S.A.

    Product code: SBF. Advisory committee: Neurology. Type: Traditional

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoAmbulatory Monitoring, Inc. — Sleep Watch (510k cleared)

    Product code: LEL. Advisory committee: Neurology. Type: Special

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoArtera, Inc. — ArteraAI Prostate (510k cleared)Arteris, Inc.

    Product code: SFH. Advisory committee: Pathology. Type: Direct

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoSiemens Medical Solutions — YSIO X.pree (510k cleared)

    Product code: KPR. Advisory committee: Radiology. Type: Traditional

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoRemedi, Inc. — REMEX Xcam6 (510k cleared)

    Product code: IZL. Advisory committee: Radiology. Type: Traditional

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoShenzhen Mindray Bio-Medical Electronics Co., Ltd. — BeneVision Central Monitoring System (510k cleared)

    Product code: MSX. Advisory committee: Cardiovascular. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025approval379d agoMETHYLPREDNISOLONE — FDA approvalMEDROL

    Sponsor: SANDOZ. Form: TABLET. Route: ORAL

    full page →MEDROL →fda approvals ↗
    ›Aug 1, 2025approval379d agoMETHYLPREDNISOLONE — FDA approvalMEDROL

    Sponsor: SANDOZ. Form: TABLET. Route: ORAL

    full page →MEDROL →fda approvals ↗
    ›Aug 1, 2025approval379d agoMETHYLPREDNISOLONE — FDA approvalMEDROL

    Sponsor: SANDOZ. Form: TABLET. Route: ORAL

    full page →MEDROL →fda approvals ↗
    ›Aug 1, 2025approval379d agoNURTEC ODT (RIMEGEPANT SULFATE) — FDA approvalrimegepant sulfate ODT

    Sponsor: PFIZER. Form: TABLET, ORALLY DISINTEGRATING. Route: ORAL

    full page →rimegepant sulfate ODT →fda approvals ↗
    ›Aug 1, 2025device pma379d agoAbiomed, Inc. — Impella 5.5 with SmartAssist System; Impella CP with SmartAssist System; Impella 2.5; Impella 5.0; Impella LD; (PMA supplement)Abion Inc

    Supplement type: Normal 180 Day Track No User Fee. Product code: OZD. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Aug 1, 2025device pma379d agoAbiomed, Inc. — Impella RP System; Impella RP with SmartAssist System; Impella RP Flex with SmartAssist System; (PMA supplement)Abion Inc

    Supplement type: Normal 180 Day Track No User Fee. Product code: PYX. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Aug 1, 2025device pma379d agoMedtronic, Inc. — AFR-00004 HexaGen RF Generator (RFG) and AFR-00008 HexaPulse PF Generator (PFG) (PMA supplement)Medtronic plc

    Supplement type: Real-Time Process. Product code: QZI. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Aug 1, 2025device pma379d agoDePuy Orthopaedics, Inc. — CERAMAX CERAMIC HIP SYSTEM (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MRA. Advisory committee: OR. Decision: OK30

    full page →fda device pma ↗
    ›Aug 1, 2025device pma379d agoMedtronic Neuromodulation — InterStim™ Therapy System, Verify™ Evaluation System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: EZW. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Aug 1, 2025device pma379d agoABBOTT MEDICAL — TactiFlex™ Ablation Catheter, Sensor Enabled™ (PMA supplement)

    Supplement type: Real-Time Process. Product code: OAE. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Aug 1, 2025device pma379d agoBoston Scientific Corp — AngioJet Thrombectomy System (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: 30-Day Notice. Product code: MCX. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Aug 1, 2025device pma379d agoMedtronic Neuromodulation — InterStim™ Therapy System, Verify™ Evaluation System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: QON. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Aug 1, 2025device recall379d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Philips Azurion System configured with a 1 Phase UPS. Azurion family (R1.x, R2.x). Labeled as the following with corresponding model numbers: 1. Azurion 3 M12, Model Number 722063. 2. Azurion 3 M15, Model Number 722064. 3. Azurion 7 B12, Model Number 722067. 4. Azurion 7 B20, Model Number 722068. 5. Azurion 7 M12, Model Number 722078. 6. Azurion 7 M20, Model Number 722079. 7. Azurion 3 M12, Model Number 722221. 8. Azurion 3 M15, Model Number 722222. 9. Azurion 7 M12, Model Number 722223. 10. Azurion 7 M20, Model Number 722224. 11. Azurion 7 B12, Model Number 722225. 12. Azurion 7 B20, Model Number 722226. 13. Azurion 5 M12, Model Number 722227. 14. Azurion 5 M20, Model Number 722228. 15. Azurion 7 M20, Model Number 722282. — Reason: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible Power Supply (UPS) have the potential of shutting down and/or not starting up, if power to the system is lost. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 1, 2025device recall379d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Philips Allura System configured with a 1 Phase UPS. Allura family (R1.x, R2.x). Labeled as the following with corresponding model numbers: 1. Allura Xper FD10, Model Number 722003 2. Allura Xper FD10/10, Model Number 722005 3. Allura Xper FD20, Model Number 722006 4. Allura Xper FD20 Biplane, Model Number 722008 5. Allura Xper FD10, Model Number 722010 6. Allura Xper FD10/10, Model Number 722011 7. Allura Xper FD20, Model Number 722012 8. Allura Xper FD20 Biplane, Model Number 722013 9. Allura Xper FD20 OR Table, Model Number 722023 10. Allura Xper FD10, Model Number 722026 11. Allura Xper FD10/10, Model Number 722027 12. Allura Xper FD20, Model Number 722028 13. Allura Xper FD20/10, Model Number 722029 14. Allura Xper FD20 OR Table, Model Number 722035 15. Allura Xper FD20/20, Model Number 722038 16. Allura Xper FD20/15, Model Number 722058 17. Allura Xper FD20/15 OR Table, Model Number 722059. — Reason: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible Power Supply (UPS) have the potential of shutting down and/or not starting up, if power to the system is lost. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 1, 2025device recall379d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series. Labeled as the following with corresponding model numbers: 1. Allura Xper FD10, Model Number 722003. 2. Allura Xper FD10/10, Model Number 722005. 3. Allura Xper FD20, Model Number 722006. 4. Allura Xper FD20 Biplane, Model Number 722008. 5. Allura Xper FD10, Model Number 722010. 6. Allura Xper FD10/10, Model Number 722011. 7. Allura Xper FD20, Model Number 722012. 8. Allura Xper FD20 Biplane, Model Number 722013. 9. Allura Xper FD20 OR Table, Model Number 722023. 10. Allura Xper FD10, Model Number 722026. 11. Allura Xper FD10/10, Model Number 722027. 12. Allura Xper FD20, Model Number 722028. 13. Allura Xper FD20/10, Model Number 722029. 14. Allura Xper FD20 OR Table, Model Number 722035. 15. Allura Xper FD20/20, Model Number 722038. 16. Allura Xper FD20/15, Model Number 722058. 510(k) Numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859. — Reason: Potential that a component (air baffle) may be missing in some Nehalem FlexVision-2 PCs that are part of the Allura Xper series. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 1, 2025device 510k379d agoShenzhen Huachuangtong Industrial Co., Ltd. — IPL Hair Removal Device (HCT-1208/HCT-1208B/HCT-1208L) (510k cleared)

    Product code: OHT. Advisory committee: General, Plastic Surgery. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoDiazyme Laboratories, Inc. — Diazyme Colorimetric Lithium Assay (510k cleared)Dolby Laboratories, Inc.

    Product code: NDW. Advisory committee: Clinical Toxicology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoGe Medical Systems, LLC — Revolution Vibe (510k cleared)

    Product code: JAK. Advisory committee: Radiology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoDeka Research and Development — Sparta Infusion Set for Insulin (510k cleared)Shanghai Jiao Tong University

    Product code: FPA. Advisory committee: General Hospital. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoShandong Huge Dental Material Corporation — NOBILCAM IMPAK Disc (510k cleared)

    Product code: MQC. Advisory committee: Unknown. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoGI Windows, Inc. — Self-Forming Magnet (Flexagon Plus OTOLoc) (510k cleared)

    Product code: SAH. Advisory committee: General, Plastic Surgery. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoAIRS, Inc. — RONAVIS – FX (FX-001) (510k cleared)AIRWA INC.

    Product code: HTY. Advisory committee: Orthopedic. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoVantive US Healthcare, LLC — AK 98 Dialysis Machine (955607) (510k cleared)

    Product code: KDI. Advisory committee: Gastroenterology, Urology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoAvizor S.A. — MINI VP1 (PL67_F); MINI VP1 (PL61_F) (510k cleared)

    Product code: LRX. Advisory committee: Ophthalmic. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoEpic Medical Pte. , Ltd. — eZSURE™ Empty Fluid Container (510k cleared)

    Product code: KPE. Advisory committee: General Hospital. Type: Special

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoBeckman Coulter, Inc. — Access hsTnI (510k cleared)

    Product code: MMI. Advisory committee: Clinical Chemistry. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoExactech, Inc. — Equinoxe® Shoulder System (510k cleared)

    Product code: PHX. Advisory committee: Orthopedic. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoDk Medical Systems Co., Ltd. — INNOVISION-DXII (510k cleared)

    Product code: KPR. Advisory committee: Radiology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoPearl Diagnostics, Inc. — MycoMEIA Aspergillus Assay (510k cleared)Co-Diagnostics, Inc.

    Product code: NOM. Advisory committee: Microbiology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoDeepSight Technology, Inc. — Deepsight NeedleVue LC1 Ultrasound System (510k cleared)

    Product code: IYO. Advisory committee: Radiology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoAccess Vascular, Inc. — HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001301); HydroPICC 4Fr Single Lumen Marked catheter, 70 cm guidewire - Basic Kit (70001302); HydroPICC 4Fr Single Lumen Marked catheter - Maximal Barrier kit (70001304); HydroPICC 5Fr Dual Lumen Marked catheter, 130 cm guidewire - Basic Kit (70002301); HydroPICC 5Fr Dual Lumen Marked catheter, 70 cm guidewire - Basic Kit (70002302); HydroPICC 5Fr Dual Lumen Marked catheter - Maximal Barrier kit (70002304); Hydr (510k cleared)

    Product code: LJS. Advisory committee: General Hospital. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoAmerican Medical Endoscopy, Inc. — Strauss Surgical Cystoscopes & Hysteroscopes (STS-2040-302ASA HD-endoscope, STS-2040-302AA HD-endoscope, STS-2040-302BA HD-endoscope, STS-2040-302BSA HD-endoscope, STS-2040-302ESA HD-endoscope, STS-2040-302CA HD-endoscope, STS-2029-302AA HD-endoscope, STS-2029-302BA HD-endoscope, STS-2040-298DSA-RWF-endoscope, STS-2040-298ASA-RWF-endoscope, STS-2040-300GSA-RWF-endoscope, STS-2040-303CA-RWF-endoscope, STS-2040-280ASA-OLY-endoscope, STS-2040-280ESA-OLY-endoscope, STS-2040-283BSA-OLY-endo (510k cleared)

    Product code: FAJ. Advisory committee: Gastroenterology, Urology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 1, 2025device 510k379d agoDentalhitec — QuickSleeper 5 (510k cleared)

    Product code: EGM. Advisory committee: Dental. Type: Traditional

    full page →fda device 510k ↗

    Week of Aug 4, 2025

    5
    ›Aug 4, 2025approval376d agoOXYCODONE HYDROCHLORIDE — FDA approvalOXYCODONE HYDROCHLORIDE

    Sponsor: ASCENT PHARMS INC. Form: TABLET. Route: ORAL

    full page →OXYCODONE HYDROCHLORIDE →fda approvals ↗
    ›Aug 4, 2025device pma
    ← prev
    page 28 of 398
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    376d ago
    Acu Focus, Inc. — IC-8 Apthera Intraocular Lens (IOL) (PMA supplement)

    Supplement type: Special (Immediate Track). Product code: POE. Advisory committee: OP. Decision: APPR

    full page →fda device pma ↗
    ›Aug 4, 2025device pma376d agoOxford Immunotec, Ltd. — T-SPOT.TB TEST (PMA supplement)

    Supplement type: Real-Time Process. Product code: OJN. Advisory committee: MI. Decision: APPR

    full page →fda device pma ↗
    ›Aug 4, 2025device pma376d agoABBOTT MEDICAL — Avant (CDHFA700Q, CDHFA700T); Neutrino NxT (CDHFA800Q, CDHFA800T CDHFA600Q, CDHFA600T); Gallant (CDHFA500Q, CDHFA500T); (PMA supplement)

    Supplement type: 30-Day Notice. Product code: NIK. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Aug 4, 2025device pma376d agoSiemens Healthcare Diagnostics Products, Ltd. — IMMULITE 2000 Systems Total Antibodies to Hepatitis B Core Antigen (Anti-HBc) (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LOM. Advisory committee: MI. Decision: OK30

    full page →fda device pma ↗
    $ZBH87.97+0.93%
    $FRTRY
    $AIP
    $MDT91.62+1.15%
    $YYAI
    $PFE26.79-0.06%
    $BSX51.83+0.27%
    $DLB
    $CODX1.51000.00%